syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis
Converting alkynes into alkenes with high stereoselectivity via two consecutive C-C bond forming steps is a desirable process, yet very challenging. Here, the authors describe a dual photoredox-nickel catalytic system for the regio- and syn-selective alkylarylation of terminal alkynes with alkyl oxa...
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2018-10-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-018-06904-9 |
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doaj-c4f51708a4e34e558cb4dc711bb94cf02021-05-11T10:08:49ZengNature Publishing GroupNature Communications2041-17232018-10-01911810.1038/s41467-018-06904-9syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysisLei Guo0Fan Song1Shengqing Zhu2Huan Li3Lingling Chu4State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry, Chemical Engineering and Biotechnology, Center for Advanced Low-Dimension Materials, Donghua UniversityState Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry, Chemical Engineering and Biotechnology, Center for Advanced Low-Dimension Materials, Donghua UniversityState Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry, Chemical Engineering and Biotechnology, Center for Advanced Low-Dimension Materials, Donghua UniversityState Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry, Chemical Engineering and Biotechnology, Center for Advanced Low-Dimension Materials, Donghua UniversityState Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Chemistry, Chemical Engineering and Biotechnology, Center for Advanced Low-Dimension Materials, Donghua UniversityConverting alkynes into alkenes with high stereoselectivity via two consecutive C-C bond forming steps is a desirable process, yet very challenging. Here, the authors describe a dual photoredox-nickel catalytic system for the regio- and syn-selective alkylarylation of terminal alkynes with alkyl oxalates and aryl bromides.https://doi.org/10.1038/s41467-018-06904-9 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lei Guo Fan Song Shengqing Zhu Huan Li Lingling Chu |
spellingShingle |
Lei Guo Fan Song Shengqing Zhu Huan Li Lingling Chu syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis Nature Communications |
author_facet |
Lei Guo Fan Song Shengqing Zhu Huan Li Lingling Chu |
author_sort |
Lei Guo |
title |
syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis |
title_short |
syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis |
title_full |
syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis |
title_fullStr |
syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis |
title_full_unstemmed |
syn-Selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis |
title_sort |
syn-selective alkylarylation of terminal alkynes via the combination of photoredox and nickel catalysis |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2018-10-01 |
description |
Converting alkynes into alkenes with high stereoselectivity via two consecutive C-C bond forming steps is a desirable process, yet very challenging. Here, the authors describe a dual photoredox-nickel catalytic system for the regio- and syn-selective alkylarylation of terminal alkynes with alkyl oxalates and aryl bromides. |
url |
https://doi.org/10.1038/s41467-018-06904-9 |
work_keys_str_mv |
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1721448652065472512 |